gas chromatography-mass spectrometry (GC-MS)" target="_blank">gas chromatography-mass spectrometry (GC-MS)')">gas chromatography-mass spectrometry (GC-MS);solid phase extraction (SPE);monoethylglycinexylidide;lidocaine;metabolin;serum&prev_q=')">serum" target="_blank">')">serum
气相色谱-质谱联用法;固相萃取;单乙基甘氨酰二甲苯胺;利多卡因;代谢物;血清;固相萃取;气相色谱;质谱法;测定;利多卡因;代谢物;单乙基甘氨酰二甲苯胺;血药浓度;spectrometry;capillary;solid;phase;ex, Open Access Library" />

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色谱  2008 

Determination of monoethylglycinexylidide concentration in serum using solid phase extraction and capillary gas chromatography-mass spectrometry
固相萃取-气相色谱-质谱法测定利多卡因代谢物单乙基甘氨酰二甲苯胺的血药浓度

Keywords: gas chromatography-mass spectrometry (GC-MS)" target="_blank">gas chromatography-mass spectrometry (GC-MS)')">gas chromatography-mass spectrometry (GC-MS)&searchField=keyword">gas chromatography-mass spectrometry (GC-MS)&prev_q=gas chromatography-mass spectrometry (GC-MS)')">gas chromatography-mass spectrometry (GC-MS)" target="_blank">gas chromatography-mass spectrometry (GC-MS)')">gas chromatography-mass spectrometry (GC-MS),solid phase extraction (SPE),monoethylglycinexylidide,lidocaine,metabolin,serum" target="_blank">')">serum
气相色谱-质谱联用法&searchField=keyword">serum&prev_q=')">serum" target="_blank">')">serum
气相色谱-质谱联用法
,固相萃取,单乙基甘氨酰二甲苯胺,利多卡因,代谢物,血清,固相萃取,气相色谱,质谱法,测定,利多卡因,代谢物,单乙基甘氨酰二甲苯胺,血药浓度,spectrometry,capillary,solid,phase,ex

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Abstract:

A novel method for the determination of monoethylglycinexylidide (MEGX) (lidocaine metabolin) in serum using solid phase extraction (SPE) and capillary gas chromatography-mass spectrometry (GC-MS) was established. The serum sample was extracted with a CN-SPE column. An HP-5MS capillary column (15 m x 0.25 mm x 0.1 microm) was used. The initial temperature of the column was set at 100 degrees C, held for 1 min, then raised to 200 degrees C at 40 degrees C/min, and held at 200 degrees C for 0.5 min. The sample size was 2 microL, and the split ratio was set at 1 : 1. The carrier gas was high purity helium with a flow rate of 1.0 mL/min. The monitoring ions for the determination were m/z 58 for MEGX and m/z 86 for procaine (internal standard). The calibration curve of MEGX had good linear relationship in the range of 1.562 - 25 ng/mL ( r = 0.998 1). The limit of detection was 0.5 ng/mL. The extraction recovery ranged from 80.1% to 85.7%. The method advanced the quantitative analysis of MEGX in serum by combining rapid and efficient SPE with specific and sensitive quantitation by GC-MS.

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